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Chronic Lymphocytic LeukemiaPhase 3VENICE INCT02756611

A Study to Evaluate the Efficacy of Venetoclax Monotherapy in Relapsed/Refractory Participants With Chronic Lymphocytic Leukemia (CLL)

A Phase 3 study testing Venetoclax in people with Chronic Lymphocytic Leukemia, run by AbbVie at 67 sites in 21 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to evaluate the efficacy of venetoclax monotherapy in participants with relapsed/refractory CLL with or without the 17p deletion or TP53 mutation, including those who have received prior treatment with a B-cell receptor inhibitor. Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Chronic Lymphocytic Leukemia
What is being tested?
Venetoclax
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
258 participants
Where
67 sitesin 21 countries
Study dates
22 Jun 2016to 11 Mar 2022
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Participant has Eastern Cooperative Oncology Group (ECOG) performance score of less than or equal to 2
  • Participant has relapsed/refractory disease (received at least 1 prior therapy)
  • Participant has diagnosis of CLL that meets published 2008 Modified International Workshop for Chronic Lymphocytic Leukemia National Cancer Institute Working Group (IWCLL NCI-WG) Guidelines and:
  • has an indication for treatment according to the 2008 Modified IWCLL NCI-WG criteria
  • has clinically measurable disease (lymphocytosis greater than 5 × 10^9/L and/or palpable and measurable nodes by physical exam and/or organomegaly assessed by physical exam)
  • In addition, participants:
Show all 9Show fewer
  • with or without 17p deletion or TP53 mutation, assessed by a local laboratory in bone marrow or peripheral blood are eligible
  • may have been previously treated with a prior B-cell receptor inhibitor
  • Participant must have adequate bone marrow function, coagulation profile, renal, and hepatic function, per laboratory at Screening

Who cannot join

  • Participant has developed Richter's transformation or Prolymphocytic leukemia
  • Participant has previously received venetoclax
  • History of active malignancies other than CLL within the past 2 years prior to first dose of venetoclax, with the exception of:
  • adequately treated in situ carcinoma of the cervix uteri
  • adequately treated basal cell carcinoma or localized squamous cell carcinoma of the skin
  • previous malignancy confined and surgically resected (or treated with other modalities) with curative intent
Show all 13Show fewer
  • Participant has active and uncontrolled autoimmune cytopenias (for 2 weeks prior to Screening), including autoimmune hemolytic anemia and idiopathic thrombocytopenic purpura despite low dose corticosteroids
  • Participant has undergone an allogeneic stem cell transplant
  • Treatment with any of the following within five half-lives or 14 days (if half-life unknown) as applicable prior to the first dose of venetoclax, or clinically significant adverse effect(s)/toxicity(s) of the previous therapy have not resolved to < National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v4.03 Grade 2:
  • Any anti-cancer therapy including chemotherapy, or radiotherapy;
  • Investigational therapy, including targeted small molecule agents
  • Participant is human immunodeficiency virus (HIV) positive
  • Participant has known allergy to both xanthine oxidase inhibitors and rasburicase

Trial locations and contacts

67 sites in 21 countries.

67 sites in 21 countries

United States6 sites
  • St. Agnes Cancer Center /ID# 149782

    Baltimore, Maryland, 21229

  • Hackensack Univ Med Ctr /ID# 151574

    Hackensack, New Jersey, 07601

  • Norton Cancer Institute /ID# 149788

    Louisville, Kentucky, 40202-3700

  • West Virginia Univ School Med /ID# 151602

    Morgantown, West Virginia, 26506

  • Utah Cancer Specialists /ID# 151604

    Salt Lake City, Utah, 84106

  • Cancer Care Northwest /ID# 151605

    Spokane, Washington, 99202

Other trials in United States

Canada5 sites
  • Qe Ii Hsc /Id# 147460

    Halifax, Nova Scotia, B3H 1V7

  • Juravinski Cancer Clinic /ID# 149152

    Hamilton, Ontario, L8V 1C3

  • CHU de Quebec-Universite Laval /ID# 150299

    Québec, Quebec, G1R 2J6

  • Sunnybrook Health Sciences Ctr /ID# 147462

    Toronto, Ontario, M4N 3M5

  • BC Cancer Agency /ID# 153091

    Vancouver, British Columbia, V5Z 1L3

Other trials in Canada

France5 sites
  • Institut Bergonie /ID# 147482

    Bordeaux, 33076

  • CHRU de Brest - Hopital Morvan /ID# 147485

    Brest, 29200

  • CHU Dupuytren /ID# 147552

    Limoges, Franche-Comte, 87042

  • CHU de la miletrie /ID# 147484

    Poitiers, Poitou-Charentes, 86021

  • clinique Sainte Anne /ID# 147556

    Strasbourg, 67085

Other trials in France

Germany5 sites
  • Onkologische Schwerpunktpraxis /ID# 147516

    Berlin, 10707

  • Cent fuer Haematologie und Onk /ID# 147511

    Frankfurt, 60389

  • OncoResearch Lerchenfeld GmbH /ID# 164044

    Hamburg, 22081

  • Mannheimer Onkologiepraxis /ID# 147512

    Mannheim, 68161

  • Staedt. Klinikum Schwabing /ID# 147510

    Munich, 80804

Other trials in Germany

Italy5 sites
  • A.O.U. Policlinico S.Orsola-Malpighi /ID# 147505

    Bologna, Emilia-Romagna, 40138

  • ASST Grande Ospedale Metropolitano Niguarda /ID# 147503

    Milan, Lombardy, 20162

  • Ospedale San Raffaele IRCCS /ID# 147504

    Milan, 20132

  • AO Maggiore della Carita /ID# 147499

    Novara, 28100

  • AP Romano Umberto I /ID# 147500

    Rome, Lazio, 00161

Other trials in Italy

Spain5 sites
  • Hospital Santa Creu i Sant Pau /ID# 151230

    Barcelona, 08026

  • Fundacion Jimenez Diaz /ID# 151231

    Madrid, 28040

  • Hosp Univ Puerta de Hierro /ID# 147391

    Majadahonda, 28222

  • Hospital Clinico Univ de Salamanca /ID# 147392

    Salamanca, 37007

  • Hosp Clin Univ de Valencia /ID# 147396

    Valencia, 46010

Other trials in Spain

Turkey (Türkiye)5 sites
  • Ankara Univ Medical Faculty /ID# 147443

    Ankara, 6100

  • Istanbul University Istanbul Medical Faculty /ID# 156040

    Istanbul, 34093

  • Vehbi Koc vakfi Amerikan Hasta /ID# 147325

    Istanbul, 34365

  • Dokuz Eylul University /ID# 147442

    Izmir, 35340

  • Ondokuz mayis University Facul /ID# 147326

    Samsun, 55139

Other trials in Turkey (Türkiye)

United Kingdom4 sites
  • Blackpool Teaching Hosp NHS /ID# 149581

    Blackpool, FY3 8NR

  • Univ Hosp Bristol NHS Foundati /ID# 147647

    Bristol, BS2 8EG

  • Southampton General Hospital /ID# 147646

    Southampton, SO16 6YD

  • The Royal Wolverhampton NHS Tr /ID# 147945

    Wolverhampton, WV10 0QP

Other trials in United Kingdom

Austria3 sites
  • LKH-Univ. Klinikum Graz /ID# 147547

    Graz, 8036

  • LKH Salzburg and Paracelsus /ID# 147549

    Salzburg, 5020

  • Hanusch Krankenhaus der WGKK /ID# 147548

    Vienna, 1140

Other trials in Austria

Israel3 sites
  • Galilee Medical Center /ID# 159971

    Nahariya, 22100

  • Sheba Medical Center /ID# 147509

    Ramat Gan, 5262100

  • Tel Aviv Sourasky Medical Ctr /ID# 151624

    Tel Aviv, Tel Aviv, 6423906

Other trials in Israel

Switzerland3 sites
  • Ospedale Regional Bellinzona e /ID# 151232

    Bellinzona, 6501

  • Hopitaux Universitaires de Geneve /ID# 147930

    Geneva, Canton of Geneva, 1205

  • University Hospital Zurich /ID# 157910

    Zurich, Canton of Zurich, 8006

Other trials in Switzerland

Belgium2 sites
  • UZ Leuven /ID# 147387

    Leuven, 3000

  • Cliniques Universitaires Saint Luc /ID# 147388

    Woluwe-Saint-Lambert, Brussels Capital, 1200

Other trials in Belgium

Denmark2 sites
  • Aarhus University Hospital /ID# 147409

    Aarhus N, Central Jutland, 8200

  • Herlev Hospital /ID# 150183

    Herlev, Capital Region, 2730

Other trials in Denmark

Greece2 sites
  • General Hospital of Athens Laiko /ID# 147517

    Athens, Attica, 115 27

  • G. Papanikolaou Hospital /ID# 147518

    Thessaloniki, 57010

Other trials in Greece

Ireland2 sites
  • St. James's Hospital /ID# 147519

    Dublin, Dublin, D08 E9P6

  • Beaumont Hospital /ID# 147522

    Dublin, D09 XR63

Other trials in Ireland

Netherlands2 sites
  • Academisch Medisch Centrum /ID# 147494

    Amsterdam, North Holland, 1105 AZ

  • Albert Schweitzer Ziekenhuis /ID# 147495

    Dordrecht, South Holland, 3318 AT

Other trials in Netherlands

Norway2 sites
  • Haukeland University Hospital /ID# 147382

    Bergen, Hordaland, 5021

  • Rikshospitalet OUS HF /ID# 201812

    Oslo, 0450

Other trials in Norway

Portugal2 sites
  • IPO Lisboa FG, EPE /ID# 147385

    Lisbon, 1099-023

  • IPO Porto FG, EPE /ID# 147389

    Porto, 4200-072

Other trials in Portugal

Sweden2 sites
  • Skanes Universitetssjukhus Lund /ID# 147439

    Lund, Skåne County, 222 41

  • Akademiska Sjukhuset /ID# 150184

    Uppsala, Uppsala County, 751 85

Other trials in Sweden

Finland1 site
  • Turku University Hospital /ID# 147551

    Turku, 20520

Other trials in Finland

Puerto Rico1 site
  • Puerto Rico Hematology Oncolog /ID# 150003

    San Juan, 00959

Other trials in Puerto Rico

About this study

Official title: Open-Label, Single Arm, Phase 3b, Multi-Center Study Evaluating the Efficacy of Venetoclax (ABT 199) in Relapsed/Refractory Subjects With Chronic Lymphocytic Leukemia (CLL)

The purpose of this study is to evaluate the efficacy of venetoclax monotherapy in participants with relapsed/refractory CLL with or without the 17p deletion or TP53 mutation, including those who have received prior treatment with a B-cell receptor inhibitor.

Read the detailed description

Following the Screening period, all eligible participants initiate venetoclax on a once daily (QD) dosing schedule. To mitigate the risk for tumor lysis syndrome (TLS), dosing will start with a 5-week dose titration phase.

Participants may receive venetoclax for up to 2 years provided they continue to tolerate the drug, have no evidence of disease progression (based on investigator assessment), do not have unacceptable toxicity and do not meet any of the criteria for subject discontinuation. In countries where venetoclax is not commercially available, participants who continued to derive benefit after 2 years of treatment may extend their treatment for up to 2 additional years in an extended access phase. Participants in the extended access phase of this study who continue to derive benefit from venetoclax after the 2-year extension and are transferring to the venetoclax extension study, Study M19-388 (NCT03844048), may remain in Extended Access for up to 1 additional year or until the extension study is approved and initiated at the site, whichever is sooner.

Being tested
Venetoclax
Keywords
Oncology, Chronic Lymphocytic Leukemia, 17p Deletion, TP53 Mutation, Relapsed, Refractory, B-Cell receptor inhibitor
Medical subject headings
Leukemia, Lymphocytic, Chronic, B-Cell, Neoplasms, Chromosome 17 deletion, Recurrence

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • VenetoclaxDrug

    Also called ABT-199, VENCLEXTA®

    Tablets for oral administration

Study groups in NCT02756611
Study groupRoleWhat they receive
VenetoclaxExperimentalVenetoclax will be administered orally once daily (QD) beginning with a dose-titration phase. The initial venetoclax dose is 20 mg QD. After 1 week of treatment at 20 mg QD, the dose will be escalated to 50 mg QD followed by subsequent increases, each after 1 week, to 100 mg QD, 200 mg QD and the maximum dose of 400 mg QD. Participants may continue to receive venetoclax for up to 2 years provided they continue to tolerate the drug, have no evidence of disease progression (based on investigator's assessment), do not have unacceptable toxicity, and do not meet any of the criteria for discontinuation. In countries where venetoclax is not commercially available, participants who continue to derive benefit after 2 years of treatment may be able to extend their treatment for up to 2 additional years, plus one additional year until the venetoclax extension study was open, determined on a case by case basis.
Receives: Drug: Venetoclax

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Complete Remission Rate in Participants Not Previously Treated With BCRi Therapy - Primary Analysis

    Complete remission rate is defined as the percentage of participants achieving a best response of complete remission (CR) or complete remission with incomplete marrow recovery (CRi) assessed by the investigator based on 2008 Modified International Workshop for Chronic Lymphocytic Leukemia National Cancer Institute-Working Group (IWCLL NCI-WG) criteria.

    CR required all of the following:

    • Peripheral blood lymphocytes < 4000/μL
    • Absence of lymphadenopathy by physical examination and computed tomography scan
    • No hepatomegaly or splenomegaly by physical examination
    • Absence of disease or constitutional symptoms (unexplained fevers > 38°C, drenching night sweats, > 10% weight loss in last 6 months)
    • Blood counts above the following:
    • Neutrophils > 1500/μL
    • Platelets > 100,000/μL
    • Hemoglobin > 110 g/L
    • Bone marrow at least normocellular for age, < 30% lymphocytes.

    CRi was defined as for CR but with persistent cytopenia apparently unrelated to CLL but related to drug toxicity.

    Measured: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.

Secondary outcomes (10)
  1. Complete Remission Rate in Participants Previously Treated With BCRi Therapy - Primary Analysis

    Complete remission rate is defined as the percentage of participants achieving a best response of complete remission (CR) or complete remission with incomplete marrow recovery (CRi) assessed by the investigator based on 2008 modified IWCLL NCI-WG criteria.

    CR required all of the following:

    • Peripheral blood lymphocytes < 4000/μL
    • Absence of lymphadenopathy by physical examination and computed tomography scan
    • No hepatomegaly or splenomegaly by physical examination
    • Absence of disease or constitutional symptoms (unexplained fevers > 38°C, drenching night sweats, > 10% weight loss in last 6 months)
    • Blood counts above the following:
    • Neutrophils > 1500/μL
    • Platelets > 100,000/μL
    • Hemoglobin > 110 g/L
    • Bone marrow at least normocellular for age, < 30% lymphocytes

    CRi was defined as for CR but with persistent cytopenia apparently unrelated to CLL but related to drug toxicity.

    Measured: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.

  2. Overall Response Rate (ORR) - Primary Analysis

    Overall response rate was defined as the percentage of participants with an overall best response of CR, CRi, nodular partial remission (nPR), or confirmed partial remission (PR) based on the 2008 modified IWCLL NCI-WG criteria assessed by the investigator.

    CR and CRi are defined above. nPR is defined as for CR but bone marrow nodules could be identified histologically.

    For PR at least 2 of the following must be met:

    • 50% decrease in peripheral blood lymphocyte count from the Baseline value;
    • 50% reduction in lymphadenopathy;
    • 50% reduction in the size of the liver and/or spleen (if abnormal prior to therapy);

    In addition at least 1 of the following criteria must be met:

    • Neutrophils > 1,500/μL or ≥ 50% improvement over Baseline;
    • Platelets > 100,000/μL or ≥ 50% improvement over Baseline;
    • Hemoglobin > 11.0 g/dL or ≥ 50% improvement over Baseline without transfusions or exogenous growth factors.

    PR must have been confirmed at least 7 weeks later.

    Measured: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.

  3. Duration of Overall Response (DOR) - Primary Analysis

    Duration of response was defined as the time from the date of first response (CR, CRi, nPR, or PR) to the earliest date that progressive disease (PD) was objectively documented (radiographic or clinical) or death. Duration of response was analyzed by Kaplan-Meier (K-M) methodology. If a participant was still responding the data were censored at the date of the last available disease assessment prior to the data cutoff date.

    Measured: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.

  4. Time to Progression (TTP) - Primary Analysis

    Time to progression was defined as the time from the date of first dose of venetoclax to the date of earliest PD (radiographic or clinical). Participants who did not experience disease progression were censored at the date of the last available disease assessment prior to the data cutoff date; participants with no post-baseline disease assessments were censored at the first dose date plus 1 day. Time to progression was estimated using Kaplan-Meier methodology.

    Measured: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.

  5. Progression-Free Survival (PFS) - Primary Analysis

    Progression-free survival (PFS) was defined as the time from the date of first dose of venetoclax to the date of earliest PD (radiographic or clinical) or death. Participants who did not experience disease progression or death were censored at the date of the last available disease assessment prior to the data cutoff date; participants with no post-baseline tumor assessment or clinical assessment for progression were censored at the date of first dose plus 1 day. Progression-free survival was analyzed by Kaplan-Meier methodology.

    Measured: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.

  6. Overall Survival (OS) - Primary Analysis

    Overall survival (time to death) was defined as the time from the first dose date of venetoclax to the date of death. If a participant had not died the data were censored at the date when they were last known to be alive prior to the cutoff date. Overall survival was analyzed using Kaplan-Meier methodology.

    Measured: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.

  7. Change From Baseline in Functional Assessment of Cancer Therapy - Leukemia Questionnaire (FACT-Leu)

    The FACT-Leu is a 44-item, leukemia-specific questionnaire designed to assess health-related quality of life (HRQoL) and leukemia-specific symptoms using a core set of questions (Functional Assessment of Cancer Therapy-General; FACT-G), and a cancer site-specific leukemia subscale. Questions are scored on a scale from 0 (not at all) to 4 (very much).

    FACT-G consists of 27 general items divided into 4 primary HRQoL domains: Physical Well-being (PWB; 7 items; score range 0-28), Social/Family Well-being (SWB; 7 items; score range 0-28), Emotional Well-being (EWB; 6 items; score range 0-24), Functional Well-being (FWB; 7 items; score range 0-28). The leukemia subscale consists of 17 items (score range 0-68) that assess patient concerns relating to leukemia. Three summary scales were calculated: FACT-Trial Outcome Index composed of the PWB, FWB, and leukemia subscale (score range 0-124); FACT-G (score range 0-108) and the FACT-Leu Total (range 0-176). Higher scores reflect better HRQoL.

    Measured: Baseline and Weeks 48 and 108

  8. Change From Baseline in Functional Assessment of Chronic Illness Therapy - Fatigue Scale (FACIT-Fatigue)

    The FACIT-Fatigue questionnaire measures fatigue and its effect on functioning and daily activities. The FACIT-Fatigue includes 13 items answered on a 5-point rating scale based on a 7-day recall period. Scores range from 0 to 52, with lower scores reflecting greater fatigue.

    Measured: Baseline and Weeks 48 and 108

  9. Change From Baseline in EuroQoL 5 Dimension 5 Level Questionnaire (EQ-5D-5L) Health Index Score

    The EQ-5D-5L is a generic measure of health status consisting of two parts: a descriptive system consisting of 5 items and a visual analog scale (VAS).

    The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. The participant is asked to rate each dimension on 5 levels of severity (1: no problems, 2: slight problems, 3: moderate problems, 4: severe problems, 5: extreme problems).

    The scores for the 5 dimensions are used to compute a single health utility index score representing the general health status of the individual. The health index score ranges from zero (defined as a health state equivalent to being dead) to 1 (full health).

    Measured: Baseline and Weeks 48 and 108

  10. Change From Baseline in EuroQoL 5 Dimension 5 Level Questionnaire (EQ-5D-5L) Visual Analog Scale Score

    The EQ-5D-5L is a generic measure of health status consisting of two parts, a descriptive system consisting of 5 items and a visual analog scale (VAS).

    The VAS assesses the participant's self-rated overall health on a scale from 0 (worst health imaginable) to 100 (best health imaginable).

    Measured: Baseline and Weeks 48 and 108

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Apr 2016 (estimated)
  2. Study start22 Jun 2016
  3. Primary completion10 Apr 2019
  4. Study completion11 Mar 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
258 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02756611
Sponsor's protocol ID
M15-550
Other IDs
2015-003667-11, 2015
Acronym
VENICE I
Status last verified
Apr 2023
First submitted
26 Apr 2016
Last updated
10 Apr 2023
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: AbbVie is committed to responsible data sharing regarding the clinical trials we sponsor. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information (e.g., protocols and clinical study reports), as long as the trials are not part of an ongoing or planned regulatory submission. This includes requests for clinical trial data for unlicensed products and indications.
Expanded access
Available

Publications

  • Kater AP, Arslan O, Demirkan F, Herishanu Y, Ferhanoglu B, Diaz MG, Leber B, Montillo M, Panayiotidis P, Rossi D, Skarbnik A, Tempescul A, Turgut M, Mellink CH, van der Kevie-Kersemaekers AF, Lanham S, Sale B, Del Rio L, Popovic R, Chyla BJ, Busman T, Komlosi V, Wang X, Sail K, Pena GE, Vizkelety T, Forconi F. Activity of venetoclax in patients with relapsed or refractory chronic lymphocytic leukaemia: analysis of the VENICE-1 multicentre, open-label, single-arm, phase 3b trial. Lancet Oncol. 2024 Apr;25(4):463-473. doi: 10.1016/S1470-2045(24)00070-6. Epub 2024 Mar 8.

    PubMed 38467131

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Venetoclax in people with Chronic Lymphocytic Leukemia, run by AbbVie at 67 sites in 21 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 67 sites in United States, Canada, France, Germany, Italy and 16 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 4 May 2020). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Complete Remission Rate in Participants Not Previously Treated With BCRi Therapy - Primary Analysis (time frame: From first dose of study drug until the last participant completed Week 48 assessments (data cut-off date 30 June 2019); overall median time on follow-up was 23.2 months.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02756611, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Apr 2023.

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